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Article Dans Une Revue Organic Letters Année : 2009

Convenient Solution-Phase Synthesis and Conformational Studies of Novel Linear and Cyclic ,-Alternating Peptoids

Résumé

The synthesis of a novel family of peptidomimetics composed of linear and cyclic α,β-alternating peptoids is described. Oligomers consisting of up to six peptoid residues (n = 1−3) were synthesized on large scale with use of an efficient iterative solution-phase method and longer oligomers (n = 4, 5) were obtained by the coupling of appropriately protected shorter oligomers. Preliminary conformational studies of these hybrid peptoids are reported.
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hal-00422367 , version 1 (06-10-2009)

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  • HAL Id : hal-00422367 , version 1

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Thomas Hjelmgaard, Sophie Faure, Cécile Caumes, Emiliana de Santis, Alison A. Edwards, et al.. Convenient Solution-Phase Synthesis and Conformational Studies of Novel Linear and Cyclic ,-Alternating Peptoids. Organic Letters, 2009, 11, pp.4100-4103. ⟨hal-00422367⟩
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